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Collaborative Research: Mechanics of Tension-Induced Adaptation in Clathrin-Mediated Endocytosis

合作研究：网格蛋白介导的内吞作用中张力诱导的适应机制

基本信息

批准号：
1562043
负责人：
Ashutosh Agrawal
金额：
$ 24.5万
依托单位：
University of Houston
依托单位国家：
美国
项目类别：
Standard Grant
财政年份：
2016
资助国家：
美国
起止时间：
2016-06-01 至 2020-05-31
项目状态：
已结题

来源：
https://www.nsf.gov/awardsearch/showAward?AWD_ID=1562043&HistoricalAwards=false
关键词：
Collaborative Research Mechanics Tension Induced

项目摘要

Transport of macromolecules into cells occurs via a collection of pathways, commonly referred to as endocytosis. These pathways are characterized by a chain of remodeling events during which an almost flat patch of plasma membrane is transformed into a cargo-carrying closed vesicle. The most commonly used pathway is called clathrin-mediated endocytosis (CME) which is important for the exchange of lipids and proteins between the plasma membrane and organelles. As such, CME is critical for maintaining the organization of the plasma membrane and regulating various cellular processes. Recent research on CME suggests that cells sense the mechanical environment by adapting the protein machinery to ensure successful CME. How cells sense and adapt to the mechanical environment to maintain cellular transport is not well understood. The goal of this project is to gain mechanistic insights into this dynamic adaptation in cells via combined theoretical and experimental approaches. Since cells experience varied mechanical environments in different diseased states, this work can provide fundamental insights into cellular transport in diseased cells that can help facilitate the design of improved nanoparticle-based drugs.This work will offer a physical explanation for the observed "mechanosensitivity" and tension-based adaptation in clathrin-mediated endocytosis. To achieve this objective, continuum mechanics and Monte Carlo simulations of membrane-protein interactions will be complimented with high-resolution live cell and super-resolution fluorescence microscopy to test the competing explanations for assembly of membrane-associated proteins and tension-induced adaptation in CME. This study will address two major debates in the endocytosis literature. First, it will identify the energetically optimal mechanism by which clathrin drives membrane curvature. Second, it will identify the mechanism by which membrane senses tension and recruits actin filaments for driving vesicle growth. The numerical and experimental findings will quantify the extent to which the key membrane-remodeling proteins can counter tension and drive vesicle growth. Overall, these findings would reveal the general principles by which tension regulates the assembly of membrane-remodeling proteins.

大分子进入细胞的转运通过一系列途径发生，通常称为内吞作用。这些途径的特征在于一系列重塑事件，在此过程中，几乎平坦的质膜被转化为携带货物的封闭囊泡。最常用的途径称为网格蛋白介导的内吞作用（CME），其对于质膜和细胞器之间的脂质和蛋白质交换是重要的。因此，CME对于维持质膜的组织和调节各种细胞过程至关重要。最近对CME的研究表明，细胞通过适应蛋白质机制来感知机械环境，以确保成功的CME。细胞如何感知和适应机械环境以维持细胞运输尚不清楚。该项目的目标是通过理论和实验相结合的方法获得对细胞中这种动态适应的机制见解。由于细胞在不同的疾病状态下经历不同的力学环境，这项工作可以提供基本的见解，在病变细胞中的细胞运输，可以帮助促进改进的纳米药物的设计。这项工作将提供一个物理解释观察到的“mechanosensitivity”和张力为基础的适应网格蛋白介导的内吞作用。为了实现这一目标，膜与蛋白质相互作用的连续介质力学和蒙特卡罗模拟将与高分辨率活细胞和超分辨率荧光显微镜相结合，以测试对CME中膜相关蛋白质组装和张力诱导适应的竞争性解释。这项研究将解决两个主要的争论在内吞作用的文献。首先，它将确定网格蛋白驱动膜曲率的能量最佳机制。第二，它将确定膜的机制，通过它来感受张力和招募肌动蛋白丝来驱动囊泡生长。数值和实验结果将量化关键膜重塑蛋白可以对抗张力和驱动囊泡生长的程度。总的来说，这些发现将揭示张力调节膜重塑蛋白组装的一般原则。